{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["EARS","PARS","GLUPRORS"],"biotype":"protein_coding","hgnc_id":"HGNC:3418","gene_name":"glutamyl-prolyl-tRNA synthetase","omim_gene":["138295"],"alias_name":["glutamate tRNA ligase","proline tRNA ligase"],"gene_symbol":"EPRS","hgnc_symbol":"EPRS","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:220141943-220220000","ensembl_id":"ENSG00000136628"}},"GRch38":{"90":{"location":"1:219968601-220046658","ensembl_id":"ENSG00000136628"}}},"hgnc_date_symbol_changed":"1991-02-20"},"entity_type":"gene","entity_name":"EPRS","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["29576217"],"evidence":["Expert Review Amber","DD-Gene2Phenotype"],"phenotypes":["Hypomyelinating Leukodystrophy"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":["new-gene-name"],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}